Biocon arm gets UK MHRA marketing authorisation for ophthalmic drug Yesafili
It is highly similar to the reference product Eylea (aflibercept).;
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Bengaluru: Biocon Biologics Limited (BBL), a subsidiary of Biocon Ltd., has announced that MHRA, Medicines and Healthcare products Regulatory Agency in the UK, has granted marketing authorization for YESAFILI, a biosimilar of Aflibercept.
In September, YESAFILI, received marketing authorization approval from the European Commission (EC) for the European Union (EU).
YESAFILI, an ophthalmology product, is intended for the treatment of neovascular (wet AMD) age-related macular degeneration, visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO), visual impairment due to diabetic macular oedema (DME) and visual impairment due to myopic choroidal neovascularisation (myopic CNV).
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